RecruitingPhase 3NCT05625724
Aspirin for the Prevention of Preeclampsia and Pregnancy Outcomes After Assisted Reproductive Technology
Studying Preeclampsia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospital, Toulouse
- Principal Investigator
- Christophe VAYSSIERE, MDUniversity Hospital, Toulouse
- Intervention
- Aspirin(drug)
- Enrollment
- 1164 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2023 – 2026
Study locations (21)
- CHU Angers, Angers, France
- CHU Bordeaux, Bordeaux, France
- CHU Clermont-Ferrand, Clermont-Ferrand, France
- CHU Dijon-Bourgogne, Dijon, France
- CHU Lille, Lille, France
- HCL - Groupement Hospitalier Est, Hôpital Femme Mère Enfant, Lyon, France
- AP-HM Hôpital de la Conception, Marseille, France
- AP-HM Hôpital Nord, Marseille, France
- CHU Montpellier, Montpellier, France
- CHRU Nancy, Nancy, France
- CHU Nantes, Nantes, France
- CHU Nîmes, Nîmes, France
- Groupe hospitalier St Joseph, Paris, France
- Hôpital Armand - Trousseau, Paris, France
- Hôpital Cochin, Paris, France
- +6 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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